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NCT Number: NCT01275534

Symptom Experience and Self-management After Haematopoietic Stem Cell Transplantation

In the study PROVIVO, a patient reported outcome instrument consisting of items from the PRO-CTCAE item bank measuring symptom experience of long-term survivors after allogeneic hematopoietic stem cell transplantation (SCT) will be developed. The instrument development is based on cognitive patient interviews, a survey of hematology experts and a literature review. In a subsequent cross-sectional study phase, the instrument will be validated in a sample of 300 allogeneic stem cell recipients and by the use of additional self report instruments it will be possible to explore how subjective symptom experience, problems in self-management and presence of late effects are connected.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

University Hospital Basel, Basel, Switzerland

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About this study

Long-term survivors after allogeneic SCT are presumably at a life-long increased risk for developing various adverse side effects; also termed 'late effects'. Late effects may appear months or years after treatment has ended, can persist chronically and may be experienced as rather distressing and burdensome. Since most late effects are only experienced subjectively in the form of physical and mental symptoms and are seldom captured during objective clinician-based evaluations, using self-report instruments is important for the early detection, management and alleviation of these symptoms. The collection of self-report data in studies and clinical practice is strongly recommended by the National Cancer Institute (NCI): they developed a Patient-Reported Outcomes bank based on the well established Common Terminology Criteria for Adverse Events (PRO-CTCAE).

Besides managing symptoms associated with late-effects, patients with SCT are also requested to manage their emotions associated with having a chronic illness, their new life roles in order to have a meaningful, fulfilling life, and their medical regimen, in view of taking medications, smoking cessation, regularly exercising and monitoring for signs of infection. However, evidence investigating the prevalence of problems related to these complex set of self-management tasks is scarce.

Aims:

  • To translate the PRO-CTCAE items into German in a culturally-sensitive way and to develop the content of a self-report instrument measuring symptom experience after allogeneic SCT
  • To validate the newly developed scale and assess its psychometric properties
  • To examine self reported symptom experience and objective measured late effects in 300 adult survivors ≥ 1 year after SCT
  • To describe self-management behaviours in 300 adult survivors ≥ 1 year after SCT
  • To assess the relationship between symptom experience and objective burden of late effects, survivors' perception of late effects and self-management in view of managing emotions, managing new life roles and managing medical and health tasks in 300 adult survivors ≥ 1 year after allogeneic SCT

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Having received allogeneic SCT for haematological disease
  • ≥ 1 year of follow-up experience after treatment
  • Ability to understand and read German and having signed the written informed consent

Exclusion criteria

  • Patients with psychiatric illness that in the opinion of physicians prevent them from participating
  • Visual and/or hearing impairment which hinders participation in an interview/fill-out a questionnaire
  • Being illiterate
  • Actual acute care hospitalization stay at interview date
  • Terminal illness

Treatment and study plan

Primary outcomes

  1. Symptom experience

    Time frame: single measuring point at ≥ 1 year after HSCT

    Patient reported symptom experience using items of the PRO-CTCAE

Secondary outcomes

  1. Perception of late effects

    Time frame: single measuring point at ≥ 1 year after HSCT

    Brief Illness Perception Questionnaire

  2. Self-management behaviors

    Time frame: single measuring point at ≥ 1 year after HSCT

    Patient reported self-management behaviors measured by single items

  3. Self-management in view of medical and health tasks, emotional and role tasks

    Time frame: single measuring point at ≥ 1 year after HSCT

    Patient reported self-management behaviors using single items and the Hospital Anxiety and Depression Scale

  4. Objective late effects

    Time frame: single measuring point at ≥ 1 year after HSCT

    Physician graded late effects using the CTCAE criteria

Sponsors and collaborators

Lead sponsor

University Hospital, Basel, Switzerland

Other

Collaborators

  • University Hospital, Zürich
  • University of Basel

Registry information

Official study title

Patient Reported Outcomes in View of Symptom Experience of Late Effects and Self-management After Haematopoietic Stem Cell Transplantation - A Mixed Methods Study

Acronym: PROVIVO

Important dates

Study start
2010
Primary completion
2012
Study completion
2012
First posted
Jan 12, 2011
Registry last updated
Jan 17, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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